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芦荟素通过转谷氨酰胺酶诱导分化增强 B16-F10 黑素瘤细胞中顺铂的抗肿瘤活性。

Aloin enhances cisplatin antineoplastic activity in B16-F10 melanoma cells by transglutaminase-induced differentiation.

机构信息

Department of Biology, University Tor Vergata, Via della Ricerca Scientifica, 00133 Rome, Italy.

出版信息

Amino Acids. 2013 Jan;44(1):293-300. doi: 10.1007/s00726-011-1166-x. Epub 2011 Dec 3.

Abstract

Aloin, a natural anthracycline from aloe plant, is a hydroxyanthraquinone derivative shown to have antitumor properties. This study demonstrated that aloin exerted inhibition of cell proliferation, adhesion and invasion abilities of B16-F10 melanoma cells under non-cytotoxic concentrations. Furthermore, aloin induced melanoma cell differentiation through the enhancement of melanogenesis and transglutaminase activity. To improve the growth-inhibiting effect of anticancer agents, we found that the combined treatment of cells with aloin and low doses of cisplatin increases the antiproliferative activity of aloin. The results suggest that aloin possesses antineoplastic and antimetastatic properties, exerted likely through the induction of melanoma cell differentiation.

摘要

芦荟大黄素,一种来自芦荟植物的天然蒽环类化合物,是一种具有抗肿瘤特性的羟基蒽醌衍生物。本研究表明,芦荟大黄素在非细胞毒性浓度下对 B16-F10 黑色素瘤细胞的增殖、黏附和侵袭能力具有抑制作用。此外,芦荟大黄素通过增强黑色素生成和转谷氨酰胺酶活性诱导黑色素瘤细胞分化。为了提高抗癌药物的生长抑制作用,我们发现用芦荟大黄素和低剂量顺铂联合处理细胞会增加芦荟大黄素的增殖抑制活性。结果表明,芦荟大黄素具有抗肿瘤和抗转移特性,可能是通过诱导黑色素瘤细胞分化来发挥作用的。

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